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FDA 510(k)

WALLSTENT TRACHEOBRONCHIAL ENDOPROSTHESIS

K-Number: K961296 · 1996-07-10

Decision Date1996-07-10
Product CodeJCT
Advisory CommitteeSU
DecisionSubstantially Equivalent - Subject to Tracking Reg.

Device Summary

WALLSTENT TRACHEOBRONCHIAL ENDOPROSTHESIS is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific Scimed, Inc.. It received FDA 510(k) clearance on 1996-07-10 under 510(k) number K961296. The device is classified under product code JCT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent - Subject to Tracking Reg..

Frequently Asked Questions

What is the WALLSTENT TRACHEOBRONCHIAL ENDOPROSTHESIS?

WALLSTENT TRACHEOBRONCHIAL ENDOPROSTHESIS is a medical device that received FDA 510(k) clearance on 1996-07-10. The listed applicant is Boston Scientific Scimed, Inc.. The 510(k) number is K961296.

When did WALLSTENT TRACHEOBRONCHIAL ENDOPROSTHESIS receive FDA 510(k) clearance?

WALLSTENT TRACHEOBRONCHIAL ENDOPROSTHESIS received FDA 510(k) clearance on 1996-07-10, under 510(k) number K961296.

Who is the listed applicant for WALLSTENT TRACHEOBRONCHIAL ENDOPROSTHESIS?

The FDA 510(k) record lists Boston Scientific Scimed, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WALLSTENT TRACHEOBRONCHIAL ENDOPROSTHESIS?

The FDA product code for WALLSTENT TRACHEOBRONCHIAL ENDOPROSTHESIS is JCT.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Boston Scientific Scimed, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 35 devices →

Related Devices (Code: JCT)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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